Abstract: A fluid connector comprises first and second connector parts. The first connector part has a body, a passage through the body, and a cylindrical outer wall with a groove around its circumference. The second connector part has a second body, a second passage, and a plurality of arms extending from a first end of the second body, each arm comprising an inwardly extending projecting portion. The arms allow the projecting portions to engage the groove. The groove has a plurality of contiguous helical portions having alternating orientations. At least one of the connector parts comprises a magnetic portion and the other comprises a second magnetic/ferromagnetic portion. Magnetic attraction between the magnetic portion and the second magnetic/ferromagnetic portion biases the connector parts towards a fully connected configuration. Relative rotation of the connector parts causes the bodies to move away from each other.

Abstract: A combined one way inspiratory valve and expiratory release valve assembly is provided for controlling air flow in a respiratory treatment system. The valve assembly comprises a housing comprising a valve inlet, a valve outlet and at least one vent opening, and a diaphragm sealingly connected to the housing at an outer circumference of the diaphragm, wherein the diaphragm divides the housing into; a) an upstream portion, which is in fluid communication with the valve inlet, and b) a downstream portion which is in fluid communication with the valve outlet. The diaphragm has a circular, oval, elliptical or stadium shape. An inner portion of the diaphragm defines a one way inspiratory valve. An outer portion of the diaphragm defines an expiratory release valve. A method of characterising vent flow in a respiratory treatment system which includes such a valve is also described.

Abstract: A patient interface includes a plenum chamber pressurizable to a therapeutic pressure, a seal-forming structure configured to form a seal against the patient's face, and a positioning and stabilising structure configured to provide a force for maintaining the seal-forming structure in a therapeutically effective position. The patient interface also includes an RPT device connected directly to the plenum chamber. The PRT device includes an electric blower for providing airflow at the therapeutic pressure. The positioning and stabilising structure supports at least part of the weight of the RPT device. The patient interface may also include an electrical power source electrically connected to the RPT device.

Abstract: A patient interface to deliver a flow of air at a positive pressure with respect to ambient air pressure to an entrance to the patient's airways to ameliorate sleep disordered breathing includes a frame assembly and a cushion assembly configured to removably and repeatably connect to the frame assembly. The frame assembly and the cushion assembly form at least part of a plenum chamber pressurizable to a therapeutic pressure. The cushion assembly comprises a one-piece construction including a seal-forming structure configured to form a seal with a region of a patient's face surrounding the entrance to the patient's airways and a frame connection structure configured to removably and repeatably connect the cushion assembly to the frame assembly. The seal-forming structure comprises a first elastomeric material and the frame connection structure comprises a second elastomeric material, the first elastomeric material comprising a lower durometer or hardness than the second elastomeric material.

Abstract: Systems and methods are disclosed for adjusting thickness of an extrudate in an extrusion die system. A lip adjustment assembly includes an engagement member connected to a movable lip of an extrusion die and being movable in a first and second direction opposite the first direction; an actuator configured to move the engagement member in the first and second directions; a coupler connected to both the engagement member and the actuator and disposed between the engagement member and the actuator; and an insulator on the coupler and configured to impede conduction of heat from the engagement member to the actuator. When the engagement member is moved in the first direction, the movable lip is moved toward a second lip of the extrusion die, and when the engagement member is moved in the second direction, the movable lip is moved away from the second lip.

Abstract: A patient interface to deliver a flow of air at a positive pressure with respect to ambient air pressure to an entrance to the patient's airways to ameliorate sleep disordered breathing includes a frame assembly and a cushion assembly configured to removably and repeatably connect to the frame assembly. The frame assembly and the cushion assembly form at least part of a plenum chamber pressurizable to a therapeutic pressure. The cushion assembly comprises a one-piece construction including a seal-forming structure configured to form a seal with a region of a patient's face surrounding the entrance to the patient's airways and a frame connection structure configured to removably and repeatably connect the cushion assembly to the frame assembly. The seal-forming structure comprises a first elastomeric material and the frame connection structure comprises a second elastomeric material, the first elastomeric material comprising a lower durometer or hardness than the second elastomeric material.

Abstract: A patient interface includes a plenum chamber pressurisable to a therapeutic pressure, and a seal-forming structure constructed and arranged to seal with a region of a patient's face surrounding an entrance to a patient's airways. The seal-forming structure is constructed and arranged to maintain the therapeutic pressure in the plenum chamber throughout a patient's respiratory cycle in use. The patient interface also includes a positioning and stabilizing structure configured to hold the seal-forming structure in a therapeutically effective position on a patient's head. The positioning and stabilizing structure includes a rear strap arranged to contact an occiput of the patient's head. The rear strap is constructed from a first material is arranged to contact a temporal region of the patient's head, and a second material arranged to contact the occiput of the patient's head. The second material is silicone.

Abstract: A patient interface includes a plenum chamber pressurisable to a therapeutic pressure, and a seal-forming structure constructed and arranged to seal with a region of a patient's face surrounding an entrance to a patient's airways. The seal-forming structure is constructed and arranged to maintain the therapeutic pressure in the plenum chamber throughout a patient's respiratory cycle in use. The patient interface also includes a positioning and stabilizing structure configured to hold the seal-forming structure in a therapeutically effective position on a patients head. The positioning and stabilizing structure includes a rear strap arranged to contact an occiput of the patient's head. The rear strap is constructed from a first material is arranged to contact a temporal region of the patient's head, and a second material arranged to contact the occiput of the patients head. The second material is silicone.

Abstract: An extrusion die has first and second die bodies that define an extrusion cavity therebetween. The extrusion cavity has an inlet, a primary manifold that extends from the inlet along a flow direction, and an outlet that defines an elongate slot. In some examples, cavity has an intermediate chamber that extends from the primary manifold along the flow direction, the intermediate chamber having a back line and a front line that taper away from one another as they extend outwards towards opposing ends of the die. The primary manifold has a front end portion that is defined between opposing inner surfaces, at least one of inner surface tapering towards the other as it extends along the flow direction. In some examples, the inner surface has first and second curved portions that curve to provide a smoother transition from the primary manifold to a downstream chamber of the extrusion cavity.

Abstract: A patient contacting member is disclosed. The patient contacting member may be configured to releasably engage a gas delivery tube which forms part of a positioning and stabilising structure for a patient interface. The patient contacting member may comprise an elongate sleeve portion which is engageable with the gas delivery tube and a strap configured to engage a back of a patients head, in use. A system for positioning and stabilising a patient interface comprising a plurality of patient contacting members is also disclosed.

Abstract: A patient interface to deliver a flow of air at a positive pressure with respect to ambient air pressure to an entrance to the patient's airways to ameliorate sleep disordered breathing includes a frame assembly and a cushion assembly configured to removably and repeatably connect to the frame assembly. The frame assembly and the cushion assembly form at least part of a plenum chamber pressurizable to a therapeutic pressure. The cushion assembly comprises a one-piece construction including a seal-forming structure configured to form a seal with a region of a patient's face surrounding the entrance to the patient's airways and a frame connection structure configured to removably and repeatably connect the cushion assembly to the frame assembly. The seal-forming structure comprises a first elastomeric material and the frame connection structure comprises a second elastomeric material, the first elastomeric material comprising a lower durometer or hardness than the second elastomeric material.

Abstract: A patient interface includes a plenum chamber pressurisable to a therapeutic pressure, and a seal-forming structure constructed and arranged to seal with a region of a patient's face surrounding an entrance to a patients airways. The seal-forming structure is constructed and arranged to maintain the therapeutic pressure in the plenum chamber throughout a patients respiratory cycle in use. The patient interface also includes a positioning and stabilizing structure configured to hold the seal-forming structure in a therapeutically effective position on a patients head. The positioning and stabilizing structure includes a rear strap arranged to contact an occiput of the patients head. The rear strap is constructed from a first material is arranged to contact a temporal region of the patients head, and a second material arranged to contact the occiput of the patients head. The second material is silicone.

Abstract: A patient interface to deliver a flow of air at a positive pressure with respect to ambient air pressure to an entrance to the patient's airways to ameliorate sleep disordered breathing includes a frame assembly and a cushion assembly configured to removably and repeatably connect to the frame assembly. The frame assembly and the cushion assembly form at least part of a plenum chamber pressurizable to a therapeutic pressure. The cushion assembly comprises a one-piece construction including a seal-forming structure configured to form a seal with a region of a patients face surrounding the entrance to the patients airways and a frame connection structure configured to removably and repeatably connect the cushion assembly to the frame assembly. The seal-forming structure comprises a first elastomeric material and the frame connection structure comprises a second elastomeric material, the first elastomeric material comprising a lower durometer or hardness than the second elastomeric material.

Abstract: A patient interface is disclosed, comprising a chassis portion having a pair of laterally projecting connection portions configured to connect to gas delivery tubes, a seal-forming structure and a vent. The seal forming structure may comprise a central portion configured to seal in use against an inferior periphery of the patients nose and a pair of lateral posterior regions. Each lateral posterior region may comprise a decoupling portion configured to at least partially decouple the central portion from a respective one of the laterally projecting connection portions. The seal-forming structure may comprise rigidising portions, a central anterior portion having a superior portion stiffer than an inferior portion, mid-lateral anterior portions having superior portions stiffer than inferior portions, and/or a lip superior portion having an anterior portion stiffer than a posterior portion. The chassis portion may be formed from a flexible material and may comprise chassis superior reinforcing portions.

Abstract: A patient interface to deliver a flow of air at a positive pressure with respect to ambient air pressure to an entrance to the patient's airways to ameliorate sleep disordered breathing includes a frame assembly and a cushion assembly configured to removably and repeatably connect to the frame assembly. The frame assembly and the cushion assembly form at least part of a plenum chamber pressurizable to a therapeutic pressure. The cushion assembly comprises a one-piece construction including a seal-forming structure configured to form a seal with a region of a patients face surrounding the entrance to the patients airways and a frame connection structure configured to removably and repeatably connect the cushion assembly to the frame assembly. The seal-forming structure comprises a first elastomeric material and the frame connection structure comprises a second elastomeric material, the first elastomeric material comprising a lower durometer or hardness than the second elastomeric material.